Pipette tip 70.3070.305

GUDID 04066916024345

Sarstedt Aktiengesellschaft & Co.KG

User-induced pipette

• Primary Device ID: 04066916024345
• NIH Device Record Key: 12420a69-ea3d-460a-8986-1821b51bc383
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pipette tip
• Version Model Number: 70.3070.305
• Catalog Number: 70.3070.305
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 80
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04066916024345 [Unit of Use]
GS1	04066916024352 [Primary]

FDA Product Code

• JRC: Micro Pipette

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-14
• Device Publish Date: 2025-04-04

On-Brand Devices [Pipette tip]

• 04066916022105: 70.3070
• 04066916023461: 70.3070.255
• 04066916032029: 70.3070.210
• 04066916031985: 70.3070.275
• 04066916031848: 70.3070.375
• 04066916025137: 70.3070.355
• 04066916024345: 70.3070.305
• 04066916031701: 70.3070.110